Literature DB >> 18661486

Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.

Chih-Ping Chen, Yann-Jang Chen, Schu-Rern Chern, Fuu-Jen Tsai, Hung-Hung Lin, Chen-Chi Lee, Wayseen Wang.   

Abstract

Entities:  

Mesh：

Year:  2008        PMID： 18661486     DOI： 10.1002/pd.2061

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


× No keyword cloud information.
  1 in total

1.  De Novo Trisomy 1q10q23.3 Mosaicism Causes Microcephaly, Severe Developmental Delay, and Facial Dysmorphic Features but No Cardiac Anomalies.

Authors:  Shirley Lo-A-Njoe; Lars T van der Veken; Clementien Vermont; Louise Rafael-Croes; Vincent Keizer; Ron Hochstenbach; Nine Knoers; Mieke M van Haelst
Journal:  Case Rep Genet       Date:  2016-01-31
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.